1-(Difluoromethyl)-2-phenyl-1H-imidazole → HCID 178449986, compound

HRID 1083858Notes

Reaction equation

HRID 1083858 reaction equation
CC(C)(C)NS(=O)(=O)c1cncc(Br)c1.FC(F)n1ccnc1-c1ccccc1>C=C[CH2][Pd][Cl].C=C[CH2][Pd][Cl].CC(=C(c1ccccc1)c1ccccc1)P(C1CCCCC1)C1CCCCC1.CC(=O)N(C)C.CC(C)(C)C(=O)[O-].[K+]>CC(C)(C)NS(=O)(=O)c1cncc(-c2cnc(-c3ccccc3)n2C(F)F)c1

Participants

8

Reactant 2

HCID 534857661-(Difluoromethyl)-2-phenyl-1H-imidazoleHCID 617949515-Bromo-N-tert-butylpyridine-3-sulfonamide

Product 1

HCID 178449986HCID 178449986, compoundYield 0.93%

Reagents, catalysts & solvents 5

HCID 23662159Potassium TrimethylacetateReagentHCID 12010824Cy-vBRIDPCatalystHCID 178455864HCID 178455864, compoundCatalystHCID 31374DimethylacetamideSolvent3×HCID 741954,4'-Bis(1,1-dimethylethyl)-1,1'-biphenylInternal standard

Conditions

Temperature
120 °C

Workup

  1. temperatureCool to room temperature
  2. additionNo procedure recorded
  3. aliquotNo procedure recorded
  4. filtrationFilter into HPLC analysis plate · Keep liquid/mobile
  5. washwash filter with 400 microliter of acetonitrile/water (4:1)

Sources & evidence

ORD record
ord-c4cb8448ad934db5ac79dc222c095a68
Source dataset
Pd-catalyzed C-H arylation of imidazole with aryl bromide
Original link
View source

Reaction notes

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